What we offer
An independent, experienced CRO providing a bespoke service, delivering clinical excellence since 1993.
LCG Bioscience is a fully integrated clinical research facility, comprising a purpose built building which includes 46 beds, sleep unit, GMP pharmacy, clinical laboratories, facilities for radioisotope studies and archives. With all these services under one roof, LCG Bioscience can rapidly process clinical samples and streamline the clinical phase of your studies.
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Consultancy & Study Design
Our experts are ideally placed to understand your needs. Between us we have been responsible for the development of a range of small molecule and biotechnology drugs through all stages of drug development, from lead selection right through to final marketing approval. This experience ensures that we have a clear insight into the pressures that our customers face, and can tailor our services accordingly.
Since 1993 LCG Bioscience has performed a wide range of exploratory phase clinical development studies, often requiring complex clinical procedures, physiological models, special populations, or novel biomarkers. With this practical experience gained over hundreds of clinical trials LCG Bioscience has tried and tested many different approaches, and can advise on which to choose to most efficiently achieve your objectives.
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Protocol Development
The project manager at LCG, in collaboration with the clinical team, will be happy to prepare study synopses and protocols to the tight timelines that you require.
These are prepared in full compliance with ICH-GCP and incorporate all elements that are required to satisfy local regulatory and ethical requirements.
CRFs at LCG Bioscience are designed by our project management team, in collaboration with the clinical study team. This ensures a CRF that is both logical in layout and efficient in use.
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Ethics & Regulatory Approval
Our project management group can prepare all of the necessary documentation for submission to the MHRA and LREC. The ethical and regulatory approval processes run in parallel, thus speeding start up times for our clinical trials.
Our principal investigators are invited to attend ethics committee meetings. This ensures that simple queries can be dealt with at the meeting and significantly improves the likelihood of gaining a rapid approval.
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Recruitment
We ensure swift recruitment rates of healthy volunteers and patients for multiple study designs.
Our experienced recruitment team are able to interrogate our database to find volunteers and patients that match the requirements of your clinical protocol. We can also actively search for new volunteers and patients, depending on your specific population requirements. Our recruitment service includes:
- Dedicated recruitment officers
- Actively managed volunteer panels
- Contracted GP network
- Established relationships with academic units, including Cambridge University
- NHS consultants facilitating varying patient populations
- Targeted marketing and recruitment campaigns
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Data Management
We have a wealth of clinical data management experience, we work with an experienced select group of successful data management companies in order to provide you with a rapid and efficient turnaround of quality data, speeding time to production of a final study report.
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Clinical Study Phase
Each clinical study is unique, and each requires its own bespoke solution. Our study teams are hand-picked from our experienced research staff to ensure that the optimum mix of skills and experience are always available to guide the study through to a successful conclusion.
Our project managers work closely with you to ensure that the study runs to your schedule, keeping you informed at all stages of our progress.
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Final Integrated Study Report
Interpretation of emerging data is crucial to the progression of any development program. At LCG Bioscience we understand the need for a thorough, but rapid evaluation of study data. The team responsible for the conduct of a study is intimately involved in the reporting process, ensuring that the people preparing your report understand all the nuances of the data.
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Safety Laboratory Services & Biomarkers
Specialised laboratory services based in purpose-built facilities, ideally positioned within our Phase I clinical trial unit.
We have the expertise and analytical capabilities to make a real difference to your project, and bring valuable returns to your IMP development. Safety assesment can be performed on site..... www.biomarker.co.uk
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